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FDA 510(k)

POWDERED VINYL EXAMINATION GLOVE

K-Number: K983893 · 1999-06-21

Decision Date1999-06-21
Product CodeLYZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

POWDERED VINYL EXAMINATION GLOVE is the device name listed in this FDA 510(k) record. The listed applicant is Shijiazhuang Brethern Plastic Co., Ltd.. It received FDA 510(k) clearance on 1999-06-21 under 510(k) number K983893. The device is classified under product code LYZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POWDERED VINYL EXAMINATION GLOVE?

POWDERED VINYL EXAMINATION GLOVE is a medical device that received FDA 510(k) clearance on 1999-06-21. The listed applicant is Shijiazhuang Brethern Plastic Co., Ltd.. The 510(k) number is K983893.

When did POWDERED VINYL EXAMINATION GLOVE receive FDA 510(k) clearance?

POWDERED VINYL EXAMINATION GLOVE received FDA 510(k) clearance on 1999-06-21, under 510(k) number K983893.

Who is the listed applicant for POWDERED VINYL EXAMINATION GLOVE?

The FDA 510(k) record lists Shijiazhuang Brethern Plastic Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for POWDERED VINYL EXAMINATION GLOVE?

The FDA product code for POWDERED VINYL EXAMINATION GLOVE is LYZ.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Shijiazhuang Brethern Plastic Co., Ltd. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: LYZ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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